Reduced SIRT1 and SIRT2 expression promotes adipogenesis of human visceral adipose stem cells and associates with accumulation of visceral fat in human obesity
Background/Objectives The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells...
Saved in:
Published in | International Journal of Obesity Vol. 44; no. 2; pp. 307 - 319 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.02.2020
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Background/Objectives
The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals.
Methods
Human ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors.
Results
Visceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of
SIRT1
and
SIRT2
showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of
SIRT1
or
SIRT2
in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of
SIRT1
or
SIRT2
in visceral ASCs from nonobese subjects enhanced this process. Changes in
SIRT1
or
SIRT2
expression and adipocyte differentiation were paralleled by corresponding changes in
PPARG
,
CEBPA
, and other genes marking terminal adipocyte differentiation.
Conclusions
SIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. |
---|---|
AbstractList | Background/Objectives The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals. Methods Human ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors. Results Visceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG, CEBPA, and other genes marking terminal adipocyte differentiation. Conclusions SIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals. Human ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors. Visceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG, CEBPA, and other genes marking terminal adipocyte differentiation. SIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. Background/Objectives The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals. Methods Human ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors. Results Visceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG , CEBPA , and other genes marking terminal adipocyte differentiation. Conclusions SIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals.BACKGROUND/OBJECTIVESThe histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals.Human ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors.METHODSHuman ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors.Visceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG, CEBPA, and other genes marking terminal adipocyte differentiation.RESULTSVisceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG, CEBPA, and other genes marking terminal adipocyte differentiation.SIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion.CONCLUSIONSSIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals. Human ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors. Visceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG, CEBPA, and other genes marking terminal adipocyte differentiation. SIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. Background/ObjectivesThe histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in gene expression and metabolic function of visceral (V) and subcutaneous (S) adipose tissue (AT) and their resident cells, the aim of this study was to investigate the role of SIRT1 and SIRT2 in the differentiation of adipose stem cells (ASCs) isolated from SAT and VAT biopsies of nondiabetic obese and nonobese individuals.MethodsHuman ASCs were isolated from paired SAT and VAT biopsies obtained from 83 nonobese and 92 obese subjects and were differentiated in vitro. Adipogenesis was evaluated by analyzing the lipid deposition using an image processing software, and gene expression by RT-qPCR. SIRT1 and SIRT2 protein expression was modified by using recombinant adenoviral vectors.ResultsVisceral but not subcutaneous ASCs from obese subjects showed an intrinsic increase in both adipogenesis and lipid accumulation when compared with ASCs from nonobese subjects, and this was associated with reduced SIRT1 and SIRT2 mRNA and protein levels. Moreover, adipose tissue mRNA levels of SIRT1 and SIRT2 showed an inverse correlation with BMI in the visceral but not subcutaneous depot. Overexpression of SIRT1 or SIRT2 in visceral ASCs from obese subjects resulted in inhibition of adipocyte differentiation, whereas knockdown of SIRT1 or SIRT2 in visceral ASCs from nonobese subjects enhanced this process. Changes in SIRT1 or SIRT2 expression and adipocyte differentiation were paralleled by corresponding changes in PPARG, CEBPA, and other genes marking terminal adipocyte differentiation.ConclusionsSIRT1 and SIRT2 modulate the differentiation of human ASC. Reduced expression of SIRT1 and SIRT2 may enhance the differentiation capacity of visceral ASC in human obesity, fostering visceral adipose tissue expansion. |
Audience | Academic |
Author | Nigro, Pasquale Cignarelli, Angelo Capuano, Palma Porro, Stefania Genchi, Valentina Annamaria Martines, Gennaro De Fazio, Michele Laviola, Luigi Natalicchio, Annalisa Giorgino, Francesco Perrini, Sebastio Caccioppoli, Cristina |
Author_xml | – sequence: 1 givenname: Sebastio surname: Perrini fullname: Perrini, Sebastio organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 2 givenname: Stefania surname: Porro fullname: Porro, Stefania organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 3 givenname: Pasquale surname: Nigro fullname: Nigro, Pasquale organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 4 givenname: Angelo surname: Cignarelli fullname: Cignarelli, Angelo organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 5 givenname: Cristina surname: Caccioppoli fullname: Caccioppoli, Cristina organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 6 givenname: Valentina Annamaria surname: Genchi fullname: Genchi, Valentina Annamaria organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 7 givenname: Gennaro surname: Martines fullname: Martines, Gennaro organization: General Surgery and Liver Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari Aldo Moro – sequence: 8 givenname: Michele surname: De Fazio fullname: De Fazio, Michele organization: General Surgery and Liver Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari Aldo Moro – sequence: 9 givenname: Palma surname: Capuano fullname: Capuano, Palma organization: General Surgery and Liver Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari Aldo Moro – sequence: 10 givenname: Annalisa orcidid: 0000-0002-6131-7517 surname: Natalicchio fullname: Natalicchio, Annalisa organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 11 givenname: Luigi surname: Laviola fullname: Laviola, Luigi organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro – sequence: 12 givenname: Francesco orcidid: 0000-0001-7372-2678 surname: Giorgino fullname: Giorgino, Francesco email: francesco.giorgino@uniba.it organization: Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31462690$$D View this record in MEDLINE/PubMed |
BookMark | eNp9ks1u1DAUhSNURKeFB2CDLCFVbFL8Ezvxsqr4qVQJqZS15Tg3M64ce4gdoE_TV8VphpZWUGWRKPnOudcn56DY88FDUbwm-Jhg1ryPFWFClJjIEldMlPWzYkWqWpS8kvVescIM1yXmgu8XBzFeYYw5x_RFsc9IJaiQeFXcXEA3GejQ17OLS4K0X54ogl_bEWK0waPtGIaQICLd2W1Yg4doIwo92kyD9uiHjQZG7ZbPEVBMMCADzsVbPx1jMFbPBj9t2iBtzDRMTqfZO7vc6XudkPU719DmKen6ZfG81y7Cq939sPj28cPl6efy_Muns9OT89LwiqRSE9bmRFpWNcRU0HZS8w4YJYQzSYF1PW6lACZ72oMkrZBN07V1k09OjSSaHRbvFt982O8TxKSGeS3ntIcwRUVpQzmuKK8z-vYRehWm0eftFM3h1xWnvHmSYhwzSrmQ99RaO1DW9yGN2syj1YkgjPAKU56p439Q-epgsCZ3orf5_QPB0V-CDWiXNjG4aY48PgTf7Lac2gE6tR3toMdr9acgGSALYMYQ4wj9HUKwmkuolhKqXEI1l1DNAdWPNMam29-d17buSSVdlDFP8WsY70P7v-g3P3XuSA |
CitedBy_id | crossref_primary_10_3390_ijms25094785 crossref_primary_10_1007_s40618_024_02516_x crossref_primary_10_3389_fcell_2020_619888 crossref_primary_10_1155_2022_4430050 crossref_primary_10_3390_nu14153145 crossref_primary_10_1007_s40200_024_01389_4 crossref_primary_10_12677_acm_2024_1482304 crossref_primary_10_1371_journal_pone_0293217 crossref_primary_10_1080_14728222_2025_2482563 crossref_primary_10_1007_s40618_020_01255_z crossref_primary_10_3390_ijms231810460 crossref_primary_10_1016_j_tranon_2023_101815 crossref_primary_10_1007_s11357_023_00863_w crossref_primary_10_1007_s40618_020_01446_8 crossref_primary_10_1080_09712119_2023_2203725 crossref_primary_10_3390_cells9081882 crossref_primary_10_1016_j_ajpath_2022_03_014 crossref_primary_10_12677_ACREM_2023_112007 crossref_primary_10_3390_ijms21176181 crossref_primary_10_3390_ijms24032310 crossref_primary_10_3389_fphar_2020_00811 crossref_primary_10_3390_biom12081079 crossref_primary_10_1038_s41598_024_52855_1 crossref_primary_10_3389_fgene_2020_590369 crossref_primary_10_1002_ijc_33118 crossref_primary_10_1016_j_biopha_2022_112908 crossref_primary_10_1016_j_lfs_2024_122431 crossref_primary_10_1016_j_isci_2024_109711 crossref_primary_10_3390_ijms23137349 crossref_primary_10_1093_jas_skac012 crossref_primary_10_3390_ijms232415860 crossref_primary_10_3390_biology10030194 crossref_primary_10_1089_dna_2020_5517 crossref_primary_10_1016_j_lfs_2024_122537 crossref_primary_10_3389_fimmu_2022_1068986 crossref_primary_10_1016_j_orcp_2020_12_001 crossref_primary_10_1186_s12964_024_02025_7 crossref_primary_10_1038_s41366_021_01053_4 crossref_primary_10_14336_AD_2020_0216 crossref_primary_10_3390_ijms24119276 crossref_primary_10_3390_nu12113506 crossref_primary_10_3390_ijms24097925 crossref_primary_10_3390_cells12040662 crossref_primary_10_1016_j_jfca_2021_104185 crossref_primary_10_1017_S0022029920000229 crossref_primary_10_1002_hep_31773 |
Cites_doi | 10.1371/journal.pone.0057892 10.1038/nature02583 10.1016/j.diabres.2013.07.002 10.2337/db08-1770 10.1074/jbc.R114.619957 10.1152/ajpregu.00653.2001 10.1371/journal.pone.0118005 10.1016/j.cmet.2011.08.006 10.1210/en.2010-0417 10.1074/jbc.M600320200 10.2337/db14-0744 10.1038/nature06902 10.1152/ajpgi.00041.2015 10.1038/ijo.2008.78 10.1016/j.tips.2015.08.001 10.1038/nm.3324 10.2337/db11-1753 10.1016/j.molmet.2015.02.007 10.1159/000489545 10.1016/j.cmet.2013.03.008 10.1111/j.1474-9726.2007.00335.x 10.1093/emboj/16.24.7432 10.1093/hmg/ddx298 10.2337/db09-0942 10.1210/jc.2012-3416 10.1371/journal.pone.0036569 10.1093/nar/gkr984 10.1128/MCB.00992-07 10.1016/j.tem.2013.12.001 10.1016/j.cmet.2007.07.003 10.1016/j.dsx.2018.11.011 10.1038/ijo.2016.131 10.1016/j.jhep.2013.07.027 10.1210/jc.2015-3095 10.1038/nrrheum.2009.137 10.1016/j.numecd.2015.11.010 10.2337/db15-1478 10.1016/j.cmet.2013.05.020 10.1101/gad.180406.111 10.2337/diabetes.55.04.06.db05-1414 10.1007/s00125-007-0841-7 10.1016/j.cytogfr.2017.11.001 10.1016/j.bbrc.2013.10.153 10.1038/nrendo.2010.20 10.18632/oncotarget.12774 10.1172/jci.insight.94379 |
ContentType | Journal Article |
Copyright | The Author(s), under exclusive licence to Springer Nature Limited 2019 COPYRIGHT 2020 Nature Publishing Group 2019© The Author(s), under exclusive licence to Springer Nature Limited 2019 The Author(s), under exclusive licence to Springer Nature Limited 2019. |
Copyright_xml | – notice: The Author(s), under exclusive licence to Springer Nature Limited 2019 – notice: COPYRIGHT 2020 Nature Publishing Group – notice: 2019© The Author(s), under exclusive licence to Springer Nature Limited 2019 – notice: The Author(s), under exclusive licence to Springer Nature Limited 2019. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7T2 7TK 7TS 7X2 7X7 7XB 88E 88G 8AO 8C1 8FE 8FH 8FI 8FJ 8FK ABUWG AEUYN AFKRA ATCPS AZQEC BBNVY BENPR BHPHI C1K CCPQU DWQXO FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0K M0S M1P M2M M7P PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS PSYQQ Q9U 7X8 |
DOI | 10.1038/s41366-019-0436-7 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health and Safety Science Abstracts (Full archive) Neurosciences Abstracts Physical Education Index Agricultural Science Collection Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Psychology Database (Alumni) ProQuest Pharma Collection Public Health Database ProQuest SciTech Collection ProQuest Natural Science Journals Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest One Sustainability ProQuest Central UK/Ireland Agricultural & Environmental Science Collection ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection Environmental Sciences and Pollution Management ProQuest One ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Biological Sciences Agricultural Science Database Health & Medical Collection (Alumni) Medical Database Psychology Database Biological Science Database ProQuest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest One Psychology ProQuest Central Basic MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Agricultural Science Database ProQuest One Psychology ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China Physical Education Index Environmental Sciences and Pollution Management ProQuest Central ProQuest One Applied & Life Sciences ProQuest One Sustainability ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Health & Medical Research Collection Agricultural & Environmental Science Collection Biological Science Collection Health & Safety Science Abstracts ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Public Health ProQuest Biological Science Collection ProQuest Central Basic ProQuest One Academic Eastern Edition Agricultural Science Collection ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Psychology Journals (Alumni) Biological Science Database ProQuest SciTech Collection Neurosciences Abstracts ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest Psychology Journals ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic Agricultural Science Database Agricultural Science Database |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central (New) url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Public Health Diet & Clinical Nutrition Recreation & Sports |
EISSN | 1476-5497 |
EndPage | 319 |
ExternalDocumentID | A613154025 31462690 10_1038_s41366_019_0436_7 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | .55 .GJ 29J 36B 39C 5RE 7X2 7X7 8R4 8R5 A8Z ABDBF ABOCM ABUWG ACUHS ADBBV AFFNX AI. ALMA_UNASSIGNED_HOLDINGS ATCPS AZQEC B0M BAWUL BENPR BHPHI BPHCQ DIK DWQXO EAD EAP EBC EBD EBS EMB EMK EMOBN EPL ESX F5P FYUFA GNUQQ HCIFZ IAO IHR ITC J5H M0K M1P M2M MVM NAO OK1 Q2X RNT RNTTT SV3 TUS VH1 WH7 X7M ZGI ZXP ~8M AAYXX CITATION --- -Q- ..I .L3 .XZ 0R~ 1CY 2FS 2WC 4.4 406 53G 5GY 70F 88E 8AO 8C1 8FE 8FH 8FI 8FJ AACDK AAHBH AANZL AASML AATNV AAWTL AAYZH ABAKF ABAWZ ABBRH ABCQX ABDBE ABFSG ABIVO ABJNI ABLJU ABRTQ ABZZP ACAOD ACGFS ACKTT ACPRK ACRQY ACSTC ACZOJ ADHUB ADXHL AEFQL AEJRE AEMSY AENEX AEUYN AEVLU AEXYK AEZWR AFBBN AFDZB AFHIU AFKRA AFRAH AFSHS AGAYW AGHAI AGQEE AHMBA AHSBF AHWEU AIGIU AILAN AIXLP AJRNO ALFFA ALIPV AMYLF APEBS ATHPR AXYYD AYFIA BBNVY BKKNO BVXVI CCPQU CGR CS3 CUY CVF DNIVK DPUIP DU5 E3Z EBLON ECM EE. EIF EIOEI EJD FDQFY FERAY FIGPU FIZPM FSGXE HMCUK HZ~ IHW INH INR IPY IWAJR JSO JZLTJ KQ8 L7B M7P NPM NQJWS O9- OVD P2P P6G PHGZM PHGZT PJZUB PPXIY PQGLB PQQKQ PROAC PSQYO PSYQQ RNS ROL SNX SNYQT SOHCF SOJ SRMVM SWTZT TAOOD TBHMF TDRGL TEORI TR2 TSG UKHRP ~KM 3V. 7T2 7TK 7TS 7XB 8FK C1K K9. LK8 PKEHL PQEST PQUKI PRINS Q9U 7X8 |
ID | FETCH-LOGICAL-c541t-a13b038b3481c4ebd9a5de32115392e3df0b96e39f2fe91b6988db78ced2c91a3 |
IEDL.DBID | 7X7 |
ISSN | 0307-0565 1476-5497 |
IngestDate | Mon Jul 21 10:56:04 EDT 2025 Sat Aug 23 13:13:01 EDT 2025 Sat Aug 23 13:13:06 EDT 2025 Tue Jun 17 20:51:52 EDT 2025 Tue Jun 10 20:51:52 EDT 2025 Thu May 22 21:20:02 EDT 2025 Mon Jul 21 06:00:42 EDT 2025 Tue Jul 01 03:02:01 EDT 2025 Thu Apr 24 23:08:44 EDT 2025 Fri Feb 21 02:39:39 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c541t-a13b038b3481c4ebd9a5de32115392e3df0b96e39f2fe91b6988db78ced2c91a3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-6131-7517 0000-0001-7372-2678 |
OpenAccessLink | http://hdl.handle.net/11586/243012 |
PMID | 31462690 |
PQID | 2350322569 |
PQPubID | 38864 |
PageCount | 13 |
ParticipantIDs | proquest_miscellaneous_2282504257 proquest_journals_2476745258 proquest_journals_2350322569 gale_infotracmisc_A613154025 gale_infotracacademiconefile_A613154025 gale_healthsolutions_A613154025 pubmed_primary_31462690 crossref_primary_10_1038_s41366_019_0436_7 crossref_citationtrail_10_1038_s41366_019_0436_7 springer_journals_10_1038_s41366_019_0436_7 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2020-02-01 |
PublicationDateYYYYMMDD | 2020-02-01 |
PublicationDate_xml | – month: 02 year: 2020 text: 2020-02-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | London |
PublicationPlace_xml | – name: London – name: England |
PublicationSubtitle | Official journal of the International Association for the Study of Obesity |
PublicationTitle | International Journal of Obesity |
PublicationTitleAbbrev | Int J Obes |
PublicationTitleAlternate | Int J Obes (Lond) |
PublicationYear | 2020 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
References | Lindroos, Husa, Mitterer, Haschemi, Rauscher, Haas (CR1) 2013; 18 Mayoral, Osborn, McNelis, Johnson, Oh, Izquierdo (CR14) 2015; 4 Moschen, Wieser, Gerner, Bichler, Enrich, Moser (CR23) 2013; 59 Guo, Li, Tang (CR42) 2015; 290 Spalding, Arner, Westermark, Bernard, Buchholz, Bergmann (CR8) 2008; 453 Cignarelli, Perrini, Nigro, Ficarella, Barbaro, Peschechera (CR19) 2016; 26 Gomes, Fleming Outeiro, Cavadas (CR10) 2015; 36 Tchkonia, Giorgadze, Pirtskhalava, Tchoukalova, Karagiannides, Forse (CR29) 2002; 282 Jukarainen, Heinonen, Rämö, Rinnankoski-Tuikka, Rappou, Tummers (CR26) 2016; 101 Laviola, Perrini, Cignarelli, Natalicchio, Leonardini, De Stefano (CR3) 2006; 55 Perrini, Ficarella, Picardi, Cignarelli, Barbaro, Nigro (CR5) 2013; 8 Krishnan, Danzer, Simka, Ukropec, Walter, Kumpf (CR27) 2012; 26 Guan, Zhang, Gao, Bai, Zhao, Cheng (CR47) 2018; 46 Perrini, Tortosa, Natalicchio, Pacelli, Cignarelli, Palmieri (CR22) 2015; 309 Baglioni, Cantini, Poli, Francalanci, Squecco, Di Franco (CR30) 2012; 7 Permana, Nair, Lee, Luczy-Bachman, Vozarova de Courten, Tataranni (CR31) 2004; 286 Kurylowicz, Owczarz, Polosak, Jonas, Lisik, Jonas (CR16) 2016; 40 Isakson, Hammarstedt, Gustafson, Smith (CR32) 2009; 58 Bordone, Cohen, Robinson, Motta, van Veen, Czopik (CR15) 2007; 6 Chang, Guarente (CR11) 2014; 25 Arner, Westermark, Spalding, Britton, Rydén, Frisén (CR9) 2010; 59 Tran, Kahn (CR2) 2010; 6 Li, Zhao, Wu, Xia, Fang, Iwasaki (CR38) 2012; 40 Tchkonia, Thomou, Zhu, Karagiannides, Pothoulakis, Jensen (CR7) 2013; 17 Wang, Tao, Gupta, Scherer (CR36) 2013; 19 Picard, Kurtev, Chung, Topark-Ngarm, Senawong, Machado de Oliveira (CR12) 2004; 429 Landgraf, Rockstroh, Wagner, Weise, Tauscher, Schwartze (CR33) 2015; 64 Ehrlund, Mejhert, Lorente-Cebrián, Aström, Dahlman, Laurencikiene (CR46) 2013; 98 Pedersen, Ølholm, Paulsen, Bennetzen, Richelsen (CR24) 2008; 32 Cignarelli, Melchiorre, Peschechera, Conserva, Renna, Miccoli (CR18) 2010; 151 Gustafson, Gogg, Hedjazifar, Jenndahl, Hammarstedt, Smith (CR34) 2009; 297 Lee, Gesta, Boucher, Wang, Kahn (CR20) 2011; 14 Perrini, Laviola, Cignarelli, Melchiorre, De Stefano, Caccioppoli (CR4) 2008; 51 Visweswaran, Schiefer, Arfuso, Dilley, Newsholme, Dharmarajan (CR45) 2015; 10 Armoni, Harel, Karni, Chen, Bar-Yoseph, Ver (CR41) 2006; 281 Takada, Kouzmenko, Kato (CR44) 2009; 5 CR21 Wang, Qiang, Farmer (CR40) 2008; 28 Macotela, Emanuelli, Mori, Gesta, Schulz, Tseng (CR6) 2012; 61 Kursawe, Dixit, Scherer, Santoro, Narayan, Gordillo (CR35) 2016; 65 Mendes, Lelis, Santos (CR37) 2017; 38 Tanaka, Yoshida, Kishimoto, Akira (CR43) 1997; 16 Martínez-Jiménez, Cortez-Espinosa, Rodríguez-Varela, Vega-Cárdenas, Briones-Espinoza, Ruíz-Rodríguez (CR17) 2019; 13 Song, Lee, Jang, Park, Kim, Lee (CR25) 2013; 101 Jing, Gesta, Kahn (CR13) 2007; 6 Lin, Sun, Jiang, Hong, Zheng (CR39) 2013; 441 Lemos, de Oliveira, Naia, Szegö, Ramos, Pinho (CR28) 2017; 26 Zhou, Song, Peng, Zhou, Wei, Zhou (CR48) 2016; 7 E Arner (436_CR9) 2010; 59 S Perrini (436_CR22) 2015; 309 QA Wang (436_CR36) 2013; 19 J Lin (436_CR39) 2013; 441 PA Permana (436_CR31) 2004; 286 B Gustafson (436_CR34) 2009; 297 YS Song (436_CR25) 2013; 101 I Takada (436_CR44) 2009; 5 K Landgraf (436_CR33) 2015; 64 R Kursawe (436_CR35) 2016; 65 M Visweswaran (436_CR45) 2015; 10 L Guo (436_CR42) 2015; 290 P Gomes (436_CR10) 2015; 36 TT Tran (436_CR2) 2010; 6 A Kurylowicz (436_CR16) 2016; 40 436_CR21 KY Lee (436_CR20) 2011; 14 Y Macotela (436_CR6) 2012; 61 V Martínez-Jiménez (436_CR17) 2019; 13 A Cignarelli (436_CR18) 2010; 151 H-C Chang (436_CR11) 2014; 25 V Lemos (436_CR28) 2017; 26 H Guan (436_CR47) 2018; 46 F Picard (436_CR12) 2004; 429 S Baglioni (436_CR30) 2012; 7 A Ehrlund (436_CR46) 2013; 98 S Perrini (436_CR5) 2013; 8 Y Zhou (436_CR48) 2016; 7 J Lindroos (436_CR1) 2013; 18 S Perrini (436_CR4) 2008; 51 T Tanaka (436_CR43) 1997; 16 J Krishnan (436_CR27) 2012; 26 P Li (436_CR38) 2012; 40 A Cignarelli (436_CR19) 2016; 26 KL Mendes (436_CR37) 2017; 38 P Isakson (436_CR32) 2009; 58 E Jing (436_CR13) 2007; 6 L Bordone (436_CR15) 2007; 6 S Jukarainen (436_CR26) 2016; 101 KL Spalding (436_CR8) 2008; 453 AR Moschen (436_CR23) 2013; 59 T Tchkonia (436_CR29) 2002; 282 H Wang (436_CR40) 2008; 28 L Laviola (436_CR3) 2006; 55 T Tchkonia (436_CR7) 2013; 17 SB Pedersen (436_CR24) 2008; 32 M Armoni (436_CR41) 2006; 281 R Mayoral (436_CR14) 2015; 4 |
References_xml | – volume: 8 year: 2013 ident: CR5 article-title: Differences in gene expression and cytokine release profiles highlight the heterogeneity of distinct subsets of adipose tissue-derived stem cells in the subcutaneous and visceral adipose tissue in humans publication-title: PLoS ONE doi: 10.1371/journal.pone.0057892 – volume: 429 start-page: 771 year: 2004 end-page: 6 ident: CR12 article-title: Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-γ publication-title: Nature doi: 10.1038/nature02583 – volume: 101 start-page: 341 year: 2013 end-page: 8 ident: CR25 article-title: Association between low SIRT1 expression in visceral and subcutaneous adipose tissues and metabolic abnormalities in women with obesity and type 2 diabetes publication-title: Diabetes Res Clin Pract doi: 10.1016/j.diabres.2013.07.002 – volume: 58 start-page: 1550 year: 2009 end-page: 7 ident: CR32 article-title: Impaired preadipocyte differentiation in human abdominal obesity: role of wnt, tumor necrosis factor-alpha, and inflammation publication-title: Diabetes doi: 10.2337/db08-1770 – volume: 290 start-page: 755 year: 2015 end-page: 61 ident: CR42 article-title: Transcriptional regulation of adipocyte differentiation: a central role for CCAAT/enhancer-binding protein (C/EBP) β publication-title: J Biol Chem doi: 10.1074/jbc.R114.619957 – volume: 282 start-page: R1286 year: 2002 end-page: 96 ident: CR29 article-title: Fat depot origin affects adipogenesis in primary cultured and cloned human preadipocytes publication-title: Am J Physiol Regul Integr Comp Physiol doi: 10.1152/ajpregu.00653.2001 – volume: 10 year: 2015 ident: CR45 article-title: Wnt antagonist secreted frizzled-related protein 4 upregulates adipogenic differentiation in human adipose tissue-derived mesenchymal stem cells publication-title: PLoS ONE doi: 10.1371/journal.pone.0118005 – volume: 14 start-page: 491 year: 2011 end-page: 503 ident: CR20 article-title: The differential role of Hif1β/Arnt and the hypoxic response in adipose function, fibrosis, and inflammation publication-title: Cell Metab doi: 10.1016/j.cmet.2011.08.006 – volume: 151 start-page: 5255 year: 2010 end-page: 66 ident: CR18 article-title: Role of UBC9 in the regulation of the adipogenic program in 3T3-L1 adipocytes publication-title: Endocrinology doi: 10.1210/en.2010-0417 – volume: 281 start-page: 19881 year: 2006 end-page: 91 ident: CR41 article-title: FOXO1 represses peroxisome proliferator-activated receptor-γ1 and -γ2 gene promoters in primary adipocytes publication-title: J Biol Chem doi: 10.1074/jbc.M600320200 – volume: 64 start-page: 1249 year: 2015 end-page: 61 ident: CR33 article-title: Evidence of early alterations in adipose tissue biology and function and its association with obesity-related inflammation and insulin resistance in children publication-title: Diabetes doi: 10.2337/db14-0744 – volume: 286 start-page: E958 year: 2004 end-page: 62 ident: CR31 article-title: Subcutaneous abdominal preadipocyte differentiation in vitro inversely correlates with central obesity publication-title: Am J Physiol Metab – volume: 453 start-page: 783 year: 2008 end-page: 7 ident: CR8 article-title: Dynamics of fat cell turnover in humans publication-title: Nature doi: 10.1038/nature06902 – volume: 309 start-page: G826 year: 2015 end-page: 40 ident: CR22 article-title: The p66 protein controls redox signaling and oxidation-dependent DNA damage in human liver cells publication-title: Am J Physiol Gastrointest Liver Physiol doi: 10.1152/ajpgi.00041.2015 – volume: 32 start-page: 1250 year: 2008 end-page: 5 ident: CR24 article-title: Low Sirt1 expression, which is upregulated by fasting, in human adipose tissue from obese women publication-title: Int J Obes doi: 10.1038/ijo.2008.78 – volume: 36 start-page: 756 year: 2015 end-page: 68 ident: CR10 article-title: Emerging role of sirtuin 2 in the regulation of mammalian metabolism publication-title: Trends Pharmacol Sci doi: 10.1016/j.tips.2015.08.001 – volume: 19 start-page: 1338 year: 2013 end-page: 44 ident: CR36 article-title: Tracking adipogenesis during white adipose tissue development, expansion and regeneration publication-title: Nat Med doi: 10.1038/nm.3324 – volume: 61 start-page: 1691 year: 2012 end-page: 9 ident: CR6 article-title: Intrinsic differences in adipocyte precursor cells from different white fat depots publication-title: Diabetes doi: 10.2337/db11-1753 – volume: 4 start-page: 378 year: 2015 end-page: 91 ident: CR14 article-title: Adipocyte SIRT1 knockout promotes PPARγ activity, adipogenesis and insulin sensitivity in chronic-HFD and obesity publication-title: Mol Metab doi: 10.1016/j.molmet.2015.02.007 – volume: 46 start-page: 2149 year: 2018 end-page: 64 ident: CR47 article-title: Differential patterns of secreted frizzled-related protein 4 (SFRP4) in adipocyte differentiation: adipose depot specificity publication-title: Cell Physiol Biochem doi: 10.1159/000489545 – volume: 17 start-page: 644 year: 2013 end-page: 56 ident: CR7 article-title: Mechanisms and metabolic implications of regional differences among fat depots publication-title: Cell Metab doi: 10.1016/j.cmet.2013.03.008 – volume: 6 start-page: 759 year: 2007 end-page: 67 ident: CR15 article-title: SIRT1 transgenic mice show phenotypes resembling calorie restriction publication-title: Aging Cell doi: 10.1111/j.1474-9726.2007.00335.x – volume: 16 start-page: 7432 year: 1997 end-page: 43 ident: CR43 article-title: Defective adipocyte differentiation in mice lacking the C/EBPbeta and/or C/EBPdelta gene publication-title: EMBO J doi: 10.1093/emboj/16.24.7432 – volume: 26 start-page: 4105 year: 2017 end-page: 17 ident: CR28 article-title: The NAD+-dependent deacetylase SIRT2 attenuates oxidative stress and mitochondrial dysfunction and improves insulin sensitivity in hepatocytes publication-title: Hum Mol Genet doi: 10.1093/hmg/ddx298 – volume: 59 start-page: 105 year: 2010 end-page: 9 ident: CR9 article-title: Adipocyte turnover: relevance to human adipose tissue morphology publication-title: Diabetes doi: 10.2337/db09-0942 – ident: CR21 – volume: 98 start-page: E503 year: 2013 end-page: 8 ident: CR46 article-title: Characterization of the Wnt inhibitors secreted frizzled-related proteins (SFRPs) in human adipose tissue publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2012-3416 – volume: 7 year: 2012 ident: CR30 article-title: Functional differences in visceral and subcutaneous fat pads originate from differences in the adipose stem cell publication-title: PLoS ONE doi: 10.1371/journal.pone.0036569 – volume: 40 start-page: 1609 year: 2012 end-page: 20 ident: CR38 article-title: Interferon gamma (IFN-γ) disrupts energy expenditure and metabolic homeostasis by suppressing SIRT1 transcription publication-title: Nucleic Acids Res doi: 10.1093/nar/gkr984 – volume: 28 start-page: 188 year: 2008 end-page: 200 ident: CR40 article-title: Identification of a domain within peroxisome proliferator-activated receptor regulating expression of a group of genes containing fibroblast growth factor 21 that are selectively repressed by SIRT1 in adipocytes publication-title: Mol Cell Biol doi: 10.1128/MCB.00992-07 – volume: 25 start-page: 138 year: 2014 end-page: 45 ident: CR11 article-title: SIRT1 and other sirtuins in metabolism publication-title: Trends Endocrinol Metab doi: 10.1016/j.tem.2013.12.001 – volume: 6 start-page: 105 year: 2007 end-page: 14 ident: CR13 article-title: SIRT2 regulates adipocyte differentiation through FoxO1 acetylation/deacetylation publication-title: Cell Metab doi: 10.1016/j.cmet.2007.07.003 – volume: 13 start-page: 582 year: 2019 end-page: 9 ident: CR17 article-title: Altered levels of sirtuin genes (SIRT1, SIRT2, SIRT3 and SIRT6) and their target genes in adipose tissue from individual with obesity publication-title: Diabetes Metab Syndr doi: 10.1016/j.dsx.2018.11.011 – volume: 40 start-page: 1635 year: 2016 end-page: 42 ident: CR16 article-title: SIRT1 and SIRT7 expression in adipose tissues of obese and normal-weight individuals is regulated by microRNAs but not by methylation status publication-title: Int J Obes doi: 10.1038/ijo.2016.131 – volume: 59 start-page: 1315 year: 2013 end-page: 22 ident: CR23 article-title: Adipose tissue and liver expression of SIRT1, 3, and 6 increase after extensive weight loss in morbid obesity publication-title: J Hepatol doi: 10.1016/j.jhep.2013.07.027 – volume: 101 start-page: 275 year: 2016 end-page: 83 ident: CR26 article-title: Obesity is associated with low NAD+/SIRT pathway expression in adipose tissue of BMI-discordant monozygotic twins publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2015-3095 – volume: 5 start-page: 442 year: 2009 end-page: 7 ident: CR44 article-title: Wnt and PPARgamma signaling in osteoblastogenesis and adipogenesis publication-title: Nat Rev Rheumatol doi: 10.1038/nrrheum.2009.137 – volume: 26 start-page: 333 year: 2016 end-page: 44 ident: CR19 article-title: Long-acting insulin analog detemir displays reduced effects on adipocyte differentiation of human subcutaneous and visceral adipose stem cells publication-title: Nutr Metab Cardiovasc Dis doi: 10.1016/j.numecd.2015.11.010 – volume: 65 start-page: 610 year: 2016 end-page: 8 ident: CR35 article-title: A Role of the inflammasome in the low storage capacity of the abdominal subcutaneous adipose tissue in obese adolescents publication-title: Diabetes doi: 10.2337/db15-1478 – volume: 18 start-page: 62 year: 2013 end-page: 74 ident: CR1 article-title: Human but not mouse adipogenesis is critically dependent on LMO3 publication-title: Cell Metab doi: 10.1016/j.cmet.2013.05.020 – volume: 26 start-page: 259 year: 2012 end-page: 70 ident: CR27 article-title: Dietary obesity-associated Hif1α activation in adipocytes restricts fatty acid oxidation and energy expenditure via suppression of the Sirt2-NAD+ system publication-title: Genes Dev doi: 10.1101/gad.180406.111 – volume: 55 start-page: 952 year: 2006 end-page: 61 ident: CR3 article-title: Insulin signaling in human visceral and subcutaneous adipose tissue in vivo publication-title: Diabetes doi: 10.2337/diabetes.55.04.06.db05-1414 – volume: 7 start-page: 77707 year: 2016 end-page: 20 ident: CR48 article-title: SIRT1 suppresses adipogenesis by activating Wnt/β-catenin signaling in vivo and in vitro publication-title: Oncotarget – volume: 51 start-page: 155 year: 2008 end-page: 64 ident: CR4 article-title: Fat depot-related differences in gene expression, adiponectin secretion, and insulin action and signalling in human adipocytes differentiated in vitro from precursor stromal cells publication-title: Diabetologia doi: 10.1007/s00125-007-0841-7 – volume: 38 start-page: 98 year: 2017 end-page: 105 ident: CR37 article-title: Nuclear sirtuins and inflammatory signaling pathways publication-title: Cytokine Growth Factor Rev doi: 10.1016/j.cytogfr.2017.11.001 – volume: 441 start-page: 897 year: 2013 end-page: 903 ident: CR39 article-title: Sirt2 suppresses inflammatory responses in collagen-induced arthritis publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2013.10.153 – volume: 6 start-page: 195 year: 2010 end-page: 213 ident: CR2 article-title: Transplantation of adipose tissue and stem cells: role in metabolism and disease publication-title: Nat Rev Endocrinol doi: 10.1038/nrendo.2010.20 – volume: 297 start-page: E999 year: 2009 end-page: 1003 ident: CR34 article-title: Inflammation and impaired adipogenesis in hypertrophic obesity in man publication-title: Am J Physiol Metab – volume: 429 start-page: 771 year: 2004 ident: 436_CR12 publication-title: Nature doi: 10.1038/nature02583 – volume: 25 start-page: 138 year: 2014 ident: 436_CR11 publication-title: Trends Endocrinol Metab doi: 10.1016/j.tem.2013.12.001 – volume: 286 start-page: E958 year: 2004 ident: 436_CR31 publication-title: Am J Physiol Metab – volume: 26 start-page: 4105 year: 2017 ident: 436_CR28 publication-title: Hum Mol Genet doi: 10.1093/hmg/ddx298 – volume: 7 year: 2012 ident: 436_CR30 publication-title: PLoS ONE doi: 10.1371/journal.pone.0036569 – volume: 36 start-page: 756 year: 2015 ident: 436_CR10 publication-title: Trends Pharmacol Sci doi: 10.1016/j.tips.2015.08.001 – volume: 64 start-page: 1249 year: 2015 ident: 436_CR33 publication-title: Diabetes doi: 10.2337/db14-0744 – volume: 151 start-page: 5255 year: 2010 ident: 436_CR18 publication-title: Endocrinology doi: 10.1210/en.2010-0417 – volume: 281 start-page: 19881 year: 2006 ident: 436_CR41 publication-title: J Biol Chem doi: 10.1074/jbc.M600320200 – volume: 18 start-page: 62 year: 2013 ident: 436_CR1 publication-title: Cell Metab doi: 10.1016/j.cmet.2013.05.020 – volume: 5 start-page: 442 year: 2009 ident: 436_CR44 publication-title: Nat Rev Rheumatol doi: 10.1038/nrrheum.2009.137 – volume: 38 start-page: 98 year: 2017 ident: 436_CR37 publication-title: Cytokine Growth Factor Rev doi: 10.1016/j.cytogfr.2017.11.001 – volume: 65 start-page: 610 year: 2016 ident: 436_CR35 publication-title: Diabetes doi: 10.2337/db15-1478 – volume: 61 start-page: 1691 year: 2012 ident: 436_CR6 publication-title: Diabetes doi: 10.2337/db11-1753 – volume: 441 start-page: 897 year: 2013 ident: 436_CR39 publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2013.10.153 – volume: 26 start-page: 259 year: 2012 ident: 436_CR27 publication-title: Genes Dev doi: 10.1101/gad.180406.111 – volume: 40 start-page: 1635 year: 2016 ident: 436_CR16 publication-title: Int J Obes doi: 10.1038/ijo.2016.131 – volume: 98 start-page: E503 year: 2013 ident: 436_CR46 publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2012-3416 – volume: 26 start-page: 333 year: 2016 ident: 436_CR19 publication-title: Nutr Metab Cardiovasc Dis doi: 10.1016/j.numecd.2015.11.010 – volume: 59 start-page: 105 year: 2010 ident: 436_CR9 publication-title: Diabetes doi: 10.2337/db09-0942 – volume: 4 start-page: 378 year: 2015 ident: 436_CR14 publication-title: Mol Metab doi: 10.1016/j.molmet.2015.02.007 – volume: 8 year: 2013 ident: 436_CR5 publication-title: PLoS ONE doi: 10.1371/journal.pone.0057892 – volume: 297 start-page: E999 year: 2009 ident: 436_CR34 publication-title: Am J Physiol Metab – volume: 290 start-page: 755 year: 2015 ident: 436_CR42 publication-title: J Biol Chem doi: 10.1074/jbc.R114.619957 – volume: 6 start-page: 195 year: 2010 ident: 436_CR2 publication-title: Nat Rev Endocrinol doi: 10.1038/nrendo.2010.20 – volume: 40 start-page: 1609 year: 2012 ident: 436_CR38 publication-title: Nucleic Acids Res doi: 10.1093/nar/gkr984 – volume: 453 start-page: 783 year: 2008 ident: 436_CR8 publication-title: Nature doi: 10.1038/nature06902 – volume: 16 start-page: 7432 year: 1997 ident: 436_CR43 publication-title: EMBO J doi: 10.1093/emboj/16.24.7432 – volume: 17 start-page: 644 year: 2013 ident: 436_CR7 publication-title: Cell Metab doi: 10.1016/j.cmet.2013.03.008 – volume: 309 start-page: G826 year: 2015 ident: 436_CR22 publication-title: Am J Physiol Gastrointest Liver Physiol doi: 10.1152/ajpgi.00041.2015 – volume: 282 start-page: R1286 year: 2002 ident: 436_CR29 publication-title: Am J Physiol Regul Integr Comp Physiol doi: 10.1152/ajpregu.00653.2001 – volume: 7 start-page: 77707 year: 2016 ident: 436_CR48 publication-title: Oncotarget doi: 10.18632/oncotarget.12774 – volume: 14 start-page: 491 year: 2011 ident: 436_CR20 publication-title: Cell Metab doi: 10.1016/j.cmet.2011.08.006 – ident: 436_CR21 doi: 10.1172/jci.insight.94379 – volume: 51 start-page: 155 year: 2008 ident: 436_CR4 publication-title: Diabetologia doi: 10.1007/s00125-007-0841-7 – volume: 46 start-page: 2149 year: 2018 ident: 436_CR47 publication-title: Cell Physiol Biochem doi: 10.1159/000489545 – volume: 101 start-page: 275 year: 2016 ident: 436_CR26 publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2015-3095 – volume: 28 start-page: 188 year: 2008 ident: 436_CR40 publication-title: Mol Cell Biol doi: 10.1128/MCB.00992-07 – volume: 10 year: 2015 ident: 436_CR45 publication-title: PLoS ONE doi: 10.1371/journal.pone.0118005 – volume: 59 start-page: 1315 year: 2013 ident: 436_CR23 publication-title: J Hepatol doi: 10.1016/j.jhep.2013.07.027 – volume: 101 start-page: 341 year: 2013 ident: 436_CR25 publication-title: Diabetes Res Clin Pract doi: 10.1016/j.diabres.2013.07.002 – volume: 58 start-page: 1550 year: 2009 ident: 436_CR32 publication-title: Diabetes doi: 10.2337/db08-1770 – volume: 55 start-page: 952 year: 2006 ident: 436_CR3 publication-title: Diabetes doi: 10.2337/diabetes.55.04.06.db05-1414 – volume: 19 start-page: 1338 year: 2013 ident: 436_CR36 publication-title: Nat Med doi: 10.1038/nm.3324 – volume: 13 start-page: 582 year: 2019 ident: 436_CR17 publication-title: Diabetes Metab Syndr doi: 10.1016/j.dsx.2018.11.011 – volume: 6 start-page: 105 year: 2007 ident: 436_CR13 publication-title: Cell Metab doi: 10.1016/j.cmet.2007.07.003 – volume: 6 start-page: 759 year: 2007 ident: 436_CR15 publication-title: Aging Cell doi: 10.1111/j.1474-9726.2007.00335.x – volume: 32 start-page: 1250 year: 2008 ident: 436_CR24 publication-title: Int J Obes doi: 10.1038/ijo.2008.78 |
SSID | ssj0005502 ssj0033214 |
Score | 2.5101995 |
Snippet | Background/Objectives
The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light... The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of the differences in... Background/Objectives The histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light... Background/ObjectivesThe histone deacetylases SIRT1 and SIRT2 have been shown to be involved in the differentiation of rodent adipocyte precursors. In light of... |
SourceID | proquest gale pubmed crossref springer |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 307 |
SubjectTerms | 13 13/100 13/106 13/95 14 38 38/44 38/77 38/90 42 45 45/29 631/208/135 631/80/458 Accumulation Adipocytes Adipocytes - metabolism Adipogenesis Adipogenesis - physiology Adipose tissue Adipose tissues Adult Biopsy Cell differentiation Cells, Cultured Computer programs Epidemiology Expression vectors Female Gene expression Gene Knockdown Techniques Genes Health Promotion and Disease Prevention Histones Humans Image processing Internal Medicine Intra-Abdominal Fat - cytology Intra-Abdominal Fat - metabolism Lipids Male Medicine Medicine & Public Health Metabolic Diseases Middle Aged Obesity Obesity - metabolism Peroxisome proliferator-activated receptors Proteins Public Health RNA SIRT1 protein Sirtuin 1 - analysis Sirtuin 1 - genetics Sirtuin 1 - metabolism Sirtuin 2 - analysis Sirtuin 2 - genetics Sirtuin 2 - metabolism Stem cell transplantation Stem cells Stem Cells - metabolism Type 2 diabetes |
Title | Reduced SIRT1 and SIRT2 expression promotes adipogenesis of human visceral adipose stem cells and associates with accumulation of visceral fat in human obesity |
URI | https://link.springer.com/article/10.1038/s41366-019-0436-7 https://www.ncbi.nlm.nih.gov/pubmed/31462690 https://www.proquest.com/docview/2350322569 https://www.proquest.com/docview/2476745258 https://www.proquest.com/docview/2282504257 |
Volume | 44 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3ra9RAEF-0BfGL6PlotNYVREEJTbJ57Se5qz2q0EPOFu5b2FckUJPT5MT_xn_Vmc0m5xXtl1xgJ5PHzM7Ozcz-hpBXPBEZlzn3M6ECP4Y54eepkj4XipWRliK08Y7zRXp2GX9aJSsXcGtdWeVgE62h1o3CGPlxxJIAlS_l79fffewahdlV10LjNtlH6DIs6cpW2bbEIwlGLCmGHXkGVERY9ZMhxcny4xYseYp_rDFPwFI_21mkrpvqv9aqa8lTuybN75N7zpmk0176D8gtU0-I96EyHX1NHeLnFV0MgPsTcufcpdInZLJ1GIHYNjtvH5LfS4RyNZp--bi8CKmo-7OIml-uYrama1vBZ1oqdLVuvqKxrFralNT2-6M_q1ZhoKsfbg1FqGiKCYLW8hNOIYABBoGpUGrzzTURQy7j9aXoaFU7rk3fwOARuZyfXpyc-a6Hg6-SOOx8ETIJn1jifl8VG6m5SLQBWYCl5ZFhugwkTw3jZVQaHsqU57mWWQ5vGikeCvaY7NVNbQ4I1SbmGggzqWUsWAJUEZdlGcuwxGYVHgkGoRXKAZxjn42rwibaWV70ci5AzgXKucg88na8ZN2je9xE_AI1oeg3qI6WoZiCRwSOKDiPHnljKdA2wJ2VcFsc4PkRZWuH8nCHEua02h0etK1wNqUttjPg38Mx4jIlUZJ75OU4jIyxjK42zQZocKeyNdMeedIr8fjeDNbMKOWBR94NWr1l_t-P8vTmJ31G7kYYoLBl7odkr_uxMc_Bi-vkkZ2qcMxPwiOyP53PZgv4nZ0uPi__AG89Q9g |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Zb9NAEB6VVAJeEITLUOgicUhUVm2vr31AqNBWCW0iFFKpb2Yvo0jFDjjh-DX8A34jO_baIRX0rW-RdjxxMrMzszOz8wE8ZRFPmEiZm3DpuaHZE24aS-EyLmkeKMH9Ot8xGseDk_DdaXS6Ab_buzDYVtnaxNpQq1Jijnw3oJGHyhez1_MvLqJGYXW1hdBo1OJI__xujmzVq-G-ke-zIDg8mL4duBZVwJVR6C9c7lPh0VTgDVQZaqEYj5Sm5iAUmVhBU5V7gsWasjzINfNFzNJUiSSVWgWS-ZwavldgM6TmKNODzTcH4_eTVVNJ5HXTqyhiALVzGE2cEbVFVZruVsZ3xHiUx8oEjd1kzS2edw5_ecdz5draCx7ehBs2fCV7jb7dgg1d9MHZn-kFeU7sjNEzMm5H_Pfh6sgW7_vQX4WohriGV69uw68JDo_VinwYTqY-4UXzKSD6h-3RLci87hnUFeFqNi8_oXmeVaTMSY0wSL7NKomptWa50gSHUxMsSVQ1P25V0DDAtDPhUi4_W9gy5NI9n_MFmRWWa9lAJtyBk0uR713oFWWh7wNROmTKECZCiZDTyFAFTOR5KPwc4TEc8FqhZdKOVEdkj7OsLu3TNGvknBk5ZyjnLHHgZffIvJknchHxNmpC1lyJ7WxRtmdiMBP6mnDVgRc1BVoj882S20sV5v1xrtca5dYapbEicn251bbMWrEqW-25fy-HOAkqCqLUgSfdMjLGxr1Cl0tDg3eja8fgwL1GibvfTY2XDmLmObDTavWK-X__lAcXv-k2XBtMR8fZ8XB89BCuB5geqZvst6C3-LrUj0wMuRCP7cYl8PGybcUfVcl-wg |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELfGkCZeEJSvwGBG4kMCRU3sOIkfEJoo08pYhcYm9S3zV1ClkRTS8vHX8H_w1-FznJROsLe9VfLlmvbOd-e78-8QesKZyLjMeZgJFYWJ3RNhnioZcqFoSbQUsct3HE7S_ZPk3ZRNN9Dv7i4MtFV2NtEZal0ryJEPCWURKF_Kh6Vvi_gw2ns9_xLCBCmotHbjNFoVOTA_v9vjW_NqPLKyfkrI3tvjN_uhnzAQKpbEi1DEVEY0l3AbVSVGai6YNtQeipiNGwzVZSR5aigvSWl4LFOe51pmuTKaKB4LavleQVczymLYY9k0W7WXsKjHsaIwDahDZLQRB-vKqzQfNtaLpHCohxoFTcNszUGedxN_-clzhVvnD_duoOs-kMW7rebdRBumGqBgNDML_Ax7tNEzPOnA_gdo69CX8QdosApWLbEbtN7cQr-OAEbWaPxxfHQcY1G1nwg2P3y3boXnrnvQNFjo2bz-BIZ61uC6xG7WIP42axQk2drlxmCAqcZQnGgcP-GV0TKABDQWSi0_-wFmwKV_vhQLPKs817odnnAbnVyKdO-gzaquzD2EtUm4toSZ1DIRlFkqwmVZJjIuYVBGgKJOaIXy4Oow4-OscEV-mhetnAsr5wLkXGQBetE_Mm-RRS4i3gFNKNrLsb1VKnZtNGaDYBu4Bui5owC7ZL9ZCX-9wr4_IHytUW6vUVp7otaXO20rvD1ritXu-_dyAphQjLA8QI_7ZWAMLXyVqZeWBm5JOxcRoLutEve_m1p_TVIeBehlp9Ur5v_9U-5f_KY7aMtaiOL9eHLwAF0jkCdx3fbbaHPxdWke2mByIR-5XYvR6WWbiT8PNoGS |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Reduced+SIRT1+and+SIRT2+expression+promotes+adipogenesis+of+human+visceral+adipose+stem+cells+and+associates+with+accumulation+of+visceral+fat+in+human+obesity&rft.jtitle=International+Journal+of+Obesity&rft.au=Perrini%2C+Sebastio&rft.au=Porro%2C+Stefania&rft.au=Caccioppoli%2C+Cristina&rft.au=Genchi%2C+Valentina+Annamaria&rft.date=2020-02-01&rft.pub=Nature+Publishing+Group&rft.issn=0307-0565&rft.volume=44&rft.issue=2&rft.spage=307&rft_id=info:doi/10.1038%2Fs41366-019-0436-7&rft.externalDBID=n%2Fa&rft.externalDocID=A613154025 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0307-0565&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0307-0565&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0307-0565&client=summon |